HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → [2-(2-Methyl-benzo[b]thiophen-3-ylsulfanyl)-phenyl]-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 2-(2-Methyl-benzo[b]thiophen-3-ylsulfanyl)-benzoic acid methyl ester | HCID 68898083 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-(2-Methyl-benzo[b]thiophen-3-ylsulfanyl)-phenyl]-methanol | HCID 68898143 | — |
Reaction Steps
Lithium aluminum hydride (250 mg, 6.6 mmol) is added to a solution of 2-(2-methyl-benzo[b]thiophen-3-ylsulfanyl)-benzoic acid methyl ester (651 mg, 2.07 mmol) in 10 mL dry THF at 0° C. The reaction mixture is stirred for 16 hours at room temperature. The reaction is quenched with 0.5 mL water. The reaction mixture is stirred for ½ hour and 0.25 mL 15% NaOH (aq) is added. The reaction mixture is stirred for 1 hour, then 1 mL water is added and stirring is continued for another hour. The mixture is filtered, dried with MgSO4 and concentrated in vacuo to give the title compound, which is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534791B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-f8d83c6e9aa34f75b5047f67cabcd8a6 |
| Source note | uspto-grants-2009_05 |